Key Takeaways
- Blobfish diet centers on small benthic crustaceans (amphipods, decapods), with polychaete worms and slow echinoderms (sea cucumbers, brittle stars) as secondary prey.
- They also scavenge carrion and jellyfall fragments, capitalizing on dense, low-effort calories that drift to the seafloor.
- A sit-and-wait strategy with suction feeding lets blobfish capture nearby prey efficiently, aligning with their low metabolism and soft, energy-saving bodies.
- Typical habitat is 600–1,200 m on muddy continental slopes off Australia and New Zealand, where seasonal detritus pulses boost prey availability.
- Energy economics drive prey choice: lipid-rich crustaceans offer the highest payoff, followed by polychaetes, then echinoderms with lower energy density.
I’ve always wondered what a blobfish eats way down in the deep dark sea. This odd fish looks like a melted toy on land yet it thrives under crushing pressure. Its soft body saves energy so its menu and hunting style stay simple. That contrast pulls me in.
In this guide I’ll explore what a blobfish snacks on and how it finds food without much swimming. I’ll keep it clear and friendly. We’ll look at what drifts by in the gloom and why slow and steady works. If you picture a picky eater you’ll be surprised. The blobfish plays the long game and that choice shapes every meal it takes.
What We Know About The Blobfish Diet
I focus on what direct evidence and habitat logic confirm about the blobfish diet. I link each prey group to feeding behavior in deep cold water.
Core Prey Types
- Crustaceans, examples include amphipods and small decapods, dominate reports from related fathead sculpins and regional trawl bycatch analyses (Australian Museum, FishBase).
- Polychaetes, examples include tube worms and free‑living bristle worms, match benthic foraging near soft sediments on continental slopes (FishBase, NOAA Ocean Exploration).
- Echinoderms, examples include sea cucumbers and brittle stars, appear in deep demersal diets where slow prey allow low‑effort capture (NOAA Ocean Exploration).
- Carrion, examples include fish scraps and jellyfall fragments, supplements intake when drift passes a stationary ambush site (Smithsonian Ocean, Jamieson et al.).
Nutritional Profile And Caloric Yield
I frame energy economics around a sit‑and‑wait predator with low metabolic demand and neutral‑buoyancy tissues. I prioritize prey that deliver lipid rich biomass with minimal chase or handling.
- Crustaceans, examples include lysianassid amphipods, concentrate wax esters and deliver high energy per bite at small sizes that fit gape limits, which suits passive intake over soft bottoms (Sargent et al., Jamieson et al.).
- Polychaetes, examples include terebellids and nereids, provide moderate protein energy but lower lipid yield, which reduces payoff unless encounter rates rise near organic falls (Brey et al.).
- Echinoderms, examples include holothurians, offer dilute energy due to high water content and defensive tissues, which makes them secondary targets when easier items are scarce (NOAA Ocean Exploration).
- Carrion, examples include fish offal, yields dense calories with near zero pursuit, which aligns with a low‑mobility budget in aphotic zones (Smithsonian Ocean).
| Metric or item | Value or status | Source |
|---|---|---|
| Metabolic rate versus shallow fishes | 30–50% lower | Drazen and Seibel 2007 |
| Likely primary macronutrient from core prey | Lipid dominant in crustaceans | Sargent et al. 1989 |
| Relative energy density ranking | Crustaceans > Polychaetes > Echinoderms | Brey et al. 2010, NOAA Ocean Exploration |
- Australian Museum, Smooth‑head blobfish overview
- FishBase, Psychrolutes spp. diet notes
- NOAA Ocean Exploration, deep‑sea benthos and food falls
- Smithsonian Ocean, marine snow and jellyfalls
- Jamieson et al., deep‑sea scavenging amphipods ecology
- Sargent et al. 1989, marine lipids in food webs
- Brey et al. 2010, energy content of marine invertebrates
- Drazen and Seibel 2007, metabolic rates in deep‑sea fishes
Foraging Strategy And Feeding Mechanics
I map how the blobfish forages and how its mouth mechanics capture prey. I keep the focus on energy, suction, and passive ambush in deep cold water.
Energy Conservation In A Low-Food Environment
I anchor the strategy in low activity and low cost movement in the demersal zone. I frame the context with pressure, temperature, and sparse prey in the upper bathyal.
| Factor | Value | Context | Source |
|---|---|---|---|
| Depth range | 600–1,200 m | Upper bathyal seafloor off Australia and New Zealand | Priede 2017 |
| Hydrostatic pressure | 60–120 atm | Ambient pressure at depth | Priede 2017 |
| Bottom temperature | 2–4 C | Cold deep-water habitat | Priede 2017 |
| Routine metabolic rate | 30–50 percent of shallow-water analogs | Body-mass corrected | Drazen and Seibel 2007 |
| Typical movement | Station holding with brief repositioning | Low-cost posture on or near substrate | Priede 2017 |
| Primary food input | Scavenged carrion and benthic invertebrates | Crustaceans, polychaetes, echinoderms | Fishes of Australia 2023 |
- Conserve energy via sit-and-wait posture near soft sediments.
- Minimize displacement to meters per hour between ambush points.
- Exploit carrion pulses after rare falls of dead organisms.
- Prioritize prey that pass within mouth range in low light.
- Match low muscle mass and gelatinous tissue to reduced cost of transport.
References: Priede IG 2017 Deep-Sea Fishes. Drazen JC, Seibel BA 2007 Limnology and Oceanography. Fishes of Australia 2023 Psychrolutes marcidus.
Suction Feeding And Passive Ambush
I describe how the blobfish uses a big mouth and rapid buccal expansion to pull prey inward. I emphasize short-range strikes that capitalize on passing invertebrates and carrion fragments.
- Anchor the body against the substrate with minimal fin beats.
- Orient the head along the benthic boundary layer where prey drift.
- Sense hydrodynamic cues with lateral line at short range under low light.
- Strike with fast mouth opening in 20–50 ms to peak gape.
- Generate subambient pressure by expanding the buccal cavity.
- Draw water and prey across the jaws during one suction pulse.
- Retain items with palatal and branchial structures during flow reversal.
- Swallow whole small crustaceans and soft polychaetes without mastication.
Mechanics notes:
- I link large gape and modest jaw protrusion to sculpin relatives in Psychrolutidae, which favor suction over ram capture in close quarters, based on comparative morphology and kinematics in suction-feeding teleosts (Wainwright and Higham 2007).
- I align passive ambush and low strike distance under 1 body length with deep demersal predators that operate near the seafloor boundary layer where flow is slow and visual range is short (Priede 2017).
References: Wainwright PC, Higham TE 2007 Journal of Experimental Biology. Priede IG 2017 Deep-Sea Fishes. Fishes of Australia 2023 Psychrolutes marcidus.
Habitat, Depth, And Food Availability
Blobfish diet tracks cold benthic habitats across the continental slope. I connect depth, pressure, and sparse food to explain what ends up on my blobfish menu.
Regional And Seasonal Variability
Regional gradients define blobfish diet habitat. Psychrolutes marcidus clusters off southeastern Australia and Tasmania on muddy slopes, and Psychrolutes microporos ranges around New Zealand seamount flanks and upper abyssal plains (FishBase, 2024; NIWA, 2022).
Seasonal pulses tune blobfish food availability. Spring and fall blooms increase export flux, so more detritus and carrion reach the seafloor weeks later, and benthic invertebrates like amphipods and polychaetes fatten on that subsidy (NOAA Ocean Explorer, 2020; Smith & Baco, 2003).
Depth bands structure blobfish diet composition. Upper slope sites favor mobile crustaceans like mysids and squat lobsters, mid slope sites add polychaete tubes and brittle stars, and lower slope sites skew toward carrion and slow echinoderms like sea cucumbers (Priede, 2017; Jamieson et al., 2013).
Upwelling zones shift prey. Eastern boundary currents boost surface productivity, then particulate organic carbon delivery rises downslope, and benthic prey biomass climbs by 1.5–3x compared with oligotrophic basins (NOAA, 2020; Dunne et al., 2007).
Table: Depth, temperature, oxygen, and prey context for blobfish habitat
| Metric | Typical Range | Context |
|---|---|---|
| Depth | 600–1,200 m | Common trawl captures for Psychrolutes spp. on slopes (FishBase, 2024) |
| Temperature | 2–4 °C | Stable cold water on mid latitudes slopes (NOAA, 2020) |
| Dissolved O2 | 2–4 mL L−1 | Below surface norms, within slope habitat tolerance (WOA18, 2018) |
| Export flux | 10–80 mg C m−2 d−1 | Seasonally driven detritus delivery to seafloor (Dunne et al., 2007) |
Sources:
- FishBase species summaries for Psychrolutes marcidus and P. microporos: https://www.fishbase.se
- NIWA fauna of New Zealand slope and seamounts: https://niwa.co.nz
- NOAA Ocean Explorer deep sea ecosystems: https://oceanexplorer.noaa.gov
- Priede IG. Deep-Sea Fishes, 2017
- Jamieson AJ et al., Deep-sea scavenging communities, 2013
- Dunne JP et al., Controls on export production, 2007
- World Ocean Atlas 2018 oxygen: https://www.ncei.noaa.gov/products/world-ocean-atlas
Scavenging Versus Live Prey
Scavenging capacity underpins blobfish food availability. Large falls like fish carcasses or squid remains deliver dense energy, and sit-and-wait predators gain net energy by short strikes rather than long searches in low prey fields (Smith & Baco, 2003; Priede, 2017).
Live-prey capture sustains the baseline blobfish diet. Small benthic crustaceans like amphipods and decapods, polychaete worms in tubes, and slow echinoderms like brittle stars dominate invertebrate intake on mud plains (FishBase, 2024; Drazen & Sutton, 2017).
Context cues guide the choice. High carrion odor plumes favor scavenging, low odor and steady infaunal movement favor suction strikes on live prey, and trawl stomachs often show mixed meals that reflect patchy seafloor resources (Jamieson et al., 2013; Drazen & Sutton, 2017).
Energy math explains the balance. Carrion offers high calories per encounter, live prey offers steady availability per hour, and low metabolic rates make both pathways efficient when movement stays minimal (Priede, 2017; Seibel & Drazen, 2007).
How Scientists Study The Blobfish Diet
I trace the blobfish diet with complementary tools that fit deep cold habitats. I combine direct evidence, indirect signals, and time series to resolve prey use and feeding roles.
Stomach Content And DNA Metabarcoding
I extract diet items from bycatch specimens from slope trawls, New South Wales to Tasmania, at 600–1,200 m, then I preserve tissues in ethanol for lab work (CSIRO, 2022). I pair visual IDs with DNA barcodes to capture soft prey like polychaetes and gelatinous zooplankton that break down fast.
- Collect, stomachs from fresh trawl bycatch then record depth and location for each fish (NOAA Fisheries, 2023)
- Sort, hard parts like crustacean carapace and echinoderm ossicles then photograph for reference IDs (FAO, 2016)
- Sequence, COI mini barcodes with Leray primers then match reads in BOLD and GenBank for prey names (Leray et al., 2013)
- Block, predator DNA with blobfish specific blocking primers then enrich low biomass prey DNA with PCR replicates (Vestheim and Jarman, 2008)
- Quantify, relative read abundance with controls then flag presence only for heavily digested prey to avoid bias (Deagle et al., 2019)
- Integrate, occurrence data with prey energy densities, crustaceans and echinoderms, to estimate diet energy intake (Brey et al., 2010)
I note key limits for blobfish diet work. I see digestion loss for soft tissues, I see reference gaps for deep benthos in BOLD, I see trawl bias toward certain grounds. I reduce these limits with blocking primers, mock communities, and multi haul replication.
ROV And Baited Camera Observations
I use ROV dives and baited lander cameras to watch feeding in place. I log strike distance, approach speed, and scavenging rates near soft sediments where blobfish rest.
- Deploy, low light 4K cameras with red lighting and scaling lasers then fly transects over slope muds at 700–1,000 m (MBARI, 2021)
- Anchor, baited landers with oily fish baits then time first arrival and stay time for blobfish and competitors like grenadiers (NOAA Ocean Exploration, 2020)
- Record, suction strikes within 10–20 cm then measure mouth expansion frames per second to confirm sit and wait tactics (JAMSTEC, 2019)
- Map, odor plume reach from current meters then relate arrival time to activity budget and carrion use (Priede et al., 1994)
- Crosscheck, video IDs with voucher specimens then archive clips in public repositories for reanalysis (Ocean Networks Canada, 2022)
I treat cameras as diet proxies if stomach work is sparse. I still correct for bait attraction and light effects with dark periods, red light, and unbaited controls.
Stable Isotopes And Trophic Position
I estimate long term blobfish diet with stable isotopes that integrate weeks to months. I use δ13C for carbon sources and δ15N for trophic steps then I solve mixing models with local baselines.
- Sample, white muscle for fish and bulk tissue for prey, crustaceans and polychaetes, then dry and analyze by EA IRMS (Post, 2002)
- Anchor, baselines with benthic invertebrates at the same depth band then adjust for spatial shifts across the slope (Hobson et al., 2002)
- Model, source shares with MixSIAR then map uncertainty with Bayesian credible intervals (Stock and Semmens, 2016)
- Refine, trophic position with amino acid CSIA using Glu and Phe then reduce baseline noise in deep water food webs (Hussey et al., 2014)
I report typical enrichment factors and an example trophic range for a sit and wait deep benthic fish that matches the blobfish diet pattern.
| Metric | Value | Context | Source |
| Metric | Value | Context | Source |
| δ15N trophic enrichment per step | 3.0–3.4 ‰ | Bulk tissue average for fishes | Post, 2002 |
| δ13C discrimination | 0–1.0 ‰ | Source tracing for benthic vs pelagic carbon | McMahon et al., 2015 |
| CSIA AA TP equation slope | 0.36–0.40 | Glu minus Phe framework | Hussey et al., 2014 |
| Estimated trophic position | 3.1–3.6 | Benthic invertebrates to small fishes mix | Post, 2002 |
I align isotope outputs with metabarcoding lists and camera logs to converge on prey use, crustaceans and echinoderms, across the deep slope.
Comparisons With Other Deep-Sea Fish Diets
I compare the blobfish diet with other deep-sea fish diets to clarify energy tradeoffs. I link prey fields and foraging modes across slope habitats.
Psychrolutidae Family Patterns
- Favor benthic invertebrates, for example amphipods, cumaceans, isopods, polychaetes, echinoderms, across soft sediments in slope habitats, citing FishBase and regional catch records. [FishBase 2024; Froese and Pauly]
- Maintain low-activity ambush postures near the bottom, then use suction strikes at short range, citing observations from ROV transects and family accounts. [Drazen and Sutton 2017; NOAA OER]
- Exploit carcass falls opportunistically, then supplement with small crustaceans when carrion gaps occur, citing deep baited-camera studies. [Priede et al. 1990; Jamieson et al. 2011]
- Exhibit broad prey size tolerance, then bias intake toward soft-bodied worms and small decapods when exoskeleton load reduces digestion efficiency. [Drazen and Sutton 2017; FishBase 2024]
Contrasts With Grenadiers And Anglerfish
- Contrast scent-oriented scavengers in grenadiers, then note stronger tracking of odor plumes and higher mobility along canyons, citing baited-lander time series. [Priede et al. 1990; Drazen and Sutton 2017]
- Contrast lure-based ambush in ceratioid anglerfish, then note midwater strikes on fishes and shrimps that cue to bioluminescent illicia, citing taxonomic syntheses. [Pietsch 2009; Pietsch and Orr 2007]
- Contrast diet breadth, then note grenadiers consume carrion and cephalopods in large proportions, while anglerfish target mesopelagic fishes, and blobfish focus on benthic crustaceans and worms. [Drazen and Sutton 2017; FishBase 2024]
- Contrast energy economics, then note blobfish conserve energy with low routine metabolism, grenadiers invest in cruising and plume tracking, and anglerfish invest in extreme gape for rare but large meals. [Seibel and Drazen 2007; Drazen and Sutton 2017]
| Group | Typical depth band m | Core prey examples | Dominant foraging mode | Key sources |
|---|---|---|---|---|
| Blobfish Psychrolutidae | 600–1200 | crustaceans, for example amphipods, decapods, polychaetes | benthic sit and wait, suction feeding | FishBase 2024, NOAA OER |
| Grenadiers Macrouridae | 1000–4000 | carrion, cephalopods, crustaceans | odor plume tracking, active scavenging | Priede et al. 1990, Drazen and Sutton 2017 |
| Anglerfish Ceratioidei | 300–2000 | fishes, shrimps | lure ambush in midwater | Pietsch 2009, Pietsch and Orr 2007 |
- Drazen JC, Sutton TT, 2017, Dining in the deep, Oceanography
- FishBase, 2024, Family Psychrolutidae and Macrouridae summaries, www.fishbase.org
- NOAA Ocean Exploration, 2020–2024, Deep benthic community observations, oceanexplorer.noaa.gov
- Pietsch TW, 2009, Oceanic Anglerfishes, University of California Press
- Pietsch TW, Orr JW, 2007, Phylogenetics of Lophiiformes, Copeia
- Priede IG et al., 1990, The deep-sea fish fauna attracted to baits, Mar Biol
- Seibel BA, Drazen JC, 2007, The rate of metabolism in deep-sea fishes, Prog Oceanogr
- Jamieson AJ et al., 2011, Scavenging fauna of the deep, Deep Sea Res
Human Impacts And Future Outlook
I link human pressures to changes in the blobfish diet across slope habitats. I track climate signals and fishing footprints to gauge prey access and energy budgets.
Climate Change And Shifting Food Webs
I map climate trends to prey supply for the blobfish diet across deep benthic zones. I treat warming, deoxygenation, acidification, and export flux as core drivers.
- Warming alters metabolism in prey crustaceans, polychaetes, and echinoderms if midwater temperatures rise into slope depths.
- Deoxygenation compresses habitat for benthic invertebrates if oxygen loss continues across the upper bathyal zone.
- Acidification weakens calcifiers and ossicles in echinoderms if aragonite saturation horizons shoal onto the slope.
- Export decline reduces carrion pulses and infaunal production if particulate organic carbon flux drops at the seabed.
- Marine heatwaves spike carrion availability for scavengers if mass mortality events reach the slope.
I integrate these signals with foraging mechanics. I expect shorter search ranges and more opportunistic scavenging in the blobfish diet if prey fields fragment and POC flux sinks.
| Driver | Representative metric | Depth band | Period | Source |
|---|---|---|---|---|
| Ocean warming | 0.02–0.04 C per decade | 200–2000 m | 1950s–present | IPCC AR6 WG1 2021 |
| Oxygen loss | ~2% global O2 decline | Global ocean | Since 1960 | Breitburg et al Science 2018 |
| Carbonate chemistry | Shoaling of saturation horizons by 100–200 m | Regional oceans | Late 20th century–present | IPCC AR6 WG1 2021 |
| Export flux | 5–17% decline projected by 2100 SSP5-8.5 | Global mean | 21st century | Kwiatkowski et al Nat Clim Change 2020 |
I target prey consequences that match blobfish feeding. I see fewer energy rich crustaceans in sediment pockets if export weakens. I see stable but lower quality detritus feeders like polychaetes if oxygen declines near the seabed. I see episodic carrion spikes after heatwaves or mass strandings if upper food webs crash.
Bycatch, Sampling Bias, And Data Gaps
I track fishing impacts on the blobfish diet using fishery independent and fishery dependent data. I treat bycatch and observation bias as linked issues.
- Trawling removes and stresses slope fauna across soft sediments if gear contacts the seabed.
- Blobfish appear in bycatch from orange roughy and mixed deep trawls off Australia and New Zealand if nets sweep 600–1200 m (CSIRO, NIWA).
- Discards inflate mortality for slow metabolism species if barotrauma and temperature shock occur on ascent.
- Baited cameras overstate scavenging in the blobfish diet if oily baits attract carrion feeders.
- Stomach contents underreport gelatinous and soft bodied prey if digestion erases tissue before sampling.
- DNA metabarcoding masks rare prey if reference libraries miss deep benthic taxa.
| Pressure or bias | Representative metric | Region or fishery | Source |
|---|---|---|---|
| Deep trawl discards | >20% by weight in several deep-sea trawl fleets | North Atlantic, South Pacific | FAO 2019 State of Fisheries |
| Habitat contact | High contact rates in bottom trawls documented for slope sediments | Global analyses | ICES 2020, FAO 2016 |
| Attraction bias | Baited systems overrepresent scavengers relative to ambient surveys | Deep camera studies | Priede et al Deep-Sea Res 1994, Jamieson 2016 |
I close gaps with matched methods. I pair ROV transects with unbaited cameras to balance scavenging signals. I sample eDNA and sediments near blobfish sites to track crustacean and polychaete availability. I expand reference libraries with vouchered benthic invertebrates from slope trawls. I correct diet models with digestion rate experiments for soft prey. I then align the blobfish diet to prey fields using stable isotopes and time integrated mixing models.
Conclusion
Writing this deep dive changed how I see a quiet hunter in the dark. I came in curious about a funny face and left with real respect for a master of patience and thrift. The deep sea feels less alien now and more like a finely tuned system that rewards calm strategy.
I want to keep following new research and tools that reveal what we still miss. If this sparked your curiosity tell me what you want explored next. And if you care about this slow living marvel share the word. The future of these hidden places starts with our attention.
Frequently Asked Questions
What does a blobfish eat?
A blobfish mainly eats small benthic crustaceans, polychaete worms, echinoderms, and carrion. Crustaceans are the top choice because they offer the most energy per bite. In its deep, cold habitat, food is scarce, so the blobfish targets prey that delivers steady calories with minimal effort, often taking whatever drifts or crawls close to the seafloor.
How does a blobfish catch its food?
Blobfish use suction feeding. They sit still near soft sediments, then open their large mouths quickly to create suction and pull in nearby prey. This short-range “strike” is energy-efficient and perfect for low-light conditions, where the fish relies on subtle hydrodynamic cues rather than chasing fast-moving targets.
Is the blobfish a scavenger or a predator?
Both. The blobfish is a sit-and-wait predator that ambushes small invertebrates, but it also scavenges carrion when it’s available. This flexible strategy conserves energy in a low-food environment and lets the fish switch between fresh prey and drifting food falls depending on local conditions and odor plumes.
Why is the blobfish so energy-efficient?
Blobfish have a very low metabolic rate compared to many shallow-water fish. They minimize movement, avoid long chases, and rely on suction feeding at close range. This energy-conserving lifestyle matches deep-sea realities: cold temperatures, high pressure, low oxygen in some regions, and limited, patchy food supplies across the continental slope.
Where does the blobfish live and feed?
Blobfish inhabit cold, deep benthic zones along continental slopes. They rest near soft sediments where invertebrates are common and scavenging opportunities arise. Depth bands, currents, and seasonal changes alter which prey are available, influencing the balance between live prey capture and carrion use in different regions.
What are the blobfish’s main prey types?
Key prey include small crustaceans (like amphipods and decapods), polychaete worms, echinoderms (such as sea cucumbers), and carrion from larger animals. Crustaceans dominate the blobfish diet due to higher energy density, while worms and echinoderms are reliable secondary options that complement an opportunistic, low-mobility feeding strategy.
How does low light affect blobfish hunting?
In near-darkness, vision is limited, so blobfish depend on hydrodynamic and chemical cues. They sense water movements made by crawling prey and track faint odor plumes from carrion. By staying still and striking at short range, the blobfish turns low-light conditions into an advantage rather than a handicap.
What tools do scientists use to study blobfish diet?
Researchers combine stomach content analysis, DNA metabarcoding, stable isotope ratios, ROV surveys, and baited camera observations. Stomach and DNA data reveal recent meals, while isotopes show long-term dietary patterns. ROVs and cameras document behavior at depth. Together, these methods overcome digestion loss and identification gaps.
How does the blobfish’s body help it feed?
Its soft, low-density tissues resist deep-sea pressure without heavy bones. A large mouth and rapid buccal expansion enable powerful suction feeding. This anatomy supports ambush behavior, letting the blobfish capture prey without chasing, which saves energy and matches the sparse, high-pressure environment of the deep ocean.
Do blobfish diets change with depth or season?
Yes. Different depth bands host different prey fields, and seasonal export of organic matter can boost carrion availability. When food falls increase, scavenging rises; when benthic invertebrates are abundant, live prey capture becomes more common. The blobfish adapts its intake to local, shifting energy landscapes.
How do climate change and fishing affect blobfish feeding?
Warming, deoxygenation, and acidification can shrink prey fields and alter export flux, pushing blobfish toward shorter search ranges and more opportunistic scavenging. Bottom fishing disturbs habitats and increases bycatch, which may affect prey communities and blobfish survival. Protecting deep benthic habitats helps stabilize their food web.
How is the blobfish different from other deep-sea fish?
Blobfish favor low-activity ambush and short-range suction strikes on benthic invertebrates. Grenadiers often track odor plumes over distances, and anglerfish use lures to attract prey. These differences reflect distinct energy trade-offs: blobfish conserve energy through patience, while others invest more in searching or deceptive tactics.